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Acta Chirurgiae Orthopaedicae Et Traumatologiae Cechoslovaca
|
February 1, 1976
[Osteodysplasty (author's transl)]
J Vanĕk, F Losan, J Fabiánová
Casopis Lekaru Ceskych
|
March 23, 1979
[Fetal hydantoin syndrome]
F Losan, Z Salcmanová, E Seemanová
Casopis Lekaru Ceskych
|
February 21, 1986
[Dermatoglyphic findings in families with spontaneous abortions]
M Kuklík, F Losan, J Srajer, et al.
Casopis Lekaru Ceskych
|
November 16, 1984
[The significance of genetic examination in the families of children with congenital cataracts]
F Losan, Z Nýdlová, J Vydrová, et al.
Human Genetics
|
January 1, 1983
A new type of familial chromosome translocation involving 3p and 6q in two unrelated families
A Gottschall, F Losan, L Pelz, et al.
Journal of Medical Genetics
|
June 1, 1986
Freeman-Sheldon syndrome: a disorder of congenital myopathic origin?
J Vanĕk, J Janda, V Amblerová, et al.
Casopis Lekaru Ceskych
|
October 17, 1986
[The importance of a genetic examination in anhidrotic ectodermal dysplasia]
F Losan, R Chalupa, J Reischig, et al.
Ceskoslovenska Pediatrie
|
May 1, 1985
[Metabolic defects in children with fetal hydantoin syndrome]
J Liska, J Varvarovská, F Losan, et al.
Human Heredity
|
January 1, 1977
X del(q) Turner's syndrome in a 30-month-old girl
F Losan, M Macek, E Seemanová, et al.
Ceskoslovenska Neurologie a Neurochirurgie
|
September 1, 1981
[Ataxia with telangiectasia--the Louis-Bar syndrome]
F Machula, K Schwartzová, V Amblerová, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 33) with videos related to
Sort By:
Page
of 4
Acta Chirurgiae Orthopaedicae Et Traumatologiae Cechoslovaca
|
February 1, 1976
[Osteodysplasty (author's transl)]
J Vanĕk, F Losan, J Fabiánová
Casopis Lekaru Ceskych
|
March 23, 1979
[Fetal hydantoin syndrome]
F Losan, Z Salcmanová, E Seemanová
Casopis Lekaru Ceskych
|
February 21, 1986
[Dermatoglyphic findings in families with spontaneous abortions]
M Kuklík, F Losan, J Srajer, et al.
Casopis Lekaru Ceskych
|
November 16, 1984
[The significance of genetic examination in the families of children with congenital cataracts]
F Losan, Z Nýdlová, J Vydrová, et al.
Human Genetics
|
January 1, 1983
A new type of familial chromosome translocation involving 3p and 6q in two unrelated families
A Gottschall, F Losan, L Pelz, et al.
Journal of Medical Genetics
|
June 1, 1986
Freeman-Sheldon syndrome: a disorder of congenital myopathic origin?
J Vanĕk, J Janda, V Amblerová, et al.
Casopis Lekaru Ceskych
|
October 17, 1986
[The importance of a genetic examination in anhidrotic ectodermal dysplasia]
F Losan, R Chalupa, J Reischig, et al.
Ceskoslovenska Pediatrie
|
May 1, 1985
[Metabolic defects in children with fetal hydantoin syndrome]
J Liska, J Varvarovská, F Losan, et al.
Human Heredity
|
January 1, 1977
X del(q) Turner's syndrome in a 30-month-old girl
F Losan, M Macek, E Seemanová, et al.
Ceskoslovenska Neurologie a Neurochirurgie
|
September 1, 1981
[Ataxia with telangiectasia--the Louis-Bar syndrome]
F Machula, K Schwartzová, V Amblerová, et al.
Page
of 4